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Glp Jobs (NOW HIRING)

Pharmatech Associates

Pharmatech Associates is seeking an experienced GLP Auditor, Contract/Project Consultant to support upcoming audits for our clients conducting regulated nonclinical research and animal studies ...

Frontage Laboratories

QA Specialist-GLP/BIO

Exton, PA · On-site

Director BIO GLP Quality assurance Full-time Position/Job Summary: Are you ready for a role that will combine your thirst for scientific knowledge and eye for quality. Then you are the perfect fit ...

Labcorp

Lead Internal Auditor, GLP/GCP

Indianapolis, IN · On-site

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

Labcorp

Lead Internal Auditor, GLP/GCP

Indianapolis, IN · On-site

Labcorp is seeking a Lead Internal Auditor, GLP/GCP to join our team in Indianapolis, IN ! Work Schedule: Monday Through Friday 8-5 pm Job Responsibilities: The Lead Internal Auditor plays a pivotal ...

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How much do glp jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for glp in the United States is $22.90, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $19.23 per hour, depending on experience, location, and employer.

What is a GLP (Good Laboratory Practice) professional?

GLP professionals are individuals who ensure that laboratory studies are conducted in accordance with Good Laboratory Practice regulations. These standards are designed to ensure the quality, reliability, and integrity of non-clinical laboratory studies, particularly those related to the safety of pharmaceuticals, chemicals, and other products. GLP professionals may work in various roles, such as quality assurance, study direction, data management, or laboratory operations. Their responsibilities include maintaining documentation, overseeing compliance, and supporting audits or inspections. By adhering to GLP guidelines, they help ensure that data generated in the lab are credible and accepted by regulatory agencies.

What are some common challenges faced by professionals working in GLP (Good Laboratory Practice) roles, and how can they be addressed?

Professionals in GLP roles often encounter challenges such as maintaining meticulous documentation, ensuring strict protocol adherence, and staying updated with evolving regulatory standards. These responsibilities require strong attention to detail and effective time management. Collaboration with cross-functional teams, such as quality assurance and laboratory staff, is essential to ensure compliance and data integrity. Regular training and open communication channels can help address these challenges and support a smooth workflow.

What are the key skills and qualifications needed to thrive as a GLP (Good Laboratory Practice) specialist, and why are they important?

To thrive as a GLP Specialist, you need a solid background in laboratory sciences, quality assurance, and regulatory compliance, often supported by a relevant degree and experience in GLP environments. Familiarity with laboratory information management systems (LIMS), audit processes, and documentation standards is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure data integrity, regulatory compliance, and the smooth operation of laboratory processes subject to strict guidelines.

What is the difference between Glp vs Pharmacist?

AspectGlpPharmacist
Required CredentialsCertification in Good Laboratory Practice (GLP) standardsDoctor of Pharmacy (PharmD) or equivalent, licensure
Work EnvironmentLaboratories, research facilitiesPharmacies, hospitals, clinics
Industry UsageRegulatory compliance, research oversightMedication dispensing, patient care
Common Search/ComparisonGLP vs PharmacistPharmacist roles, responsibilities

GLP professionals focus on ensuring laboratory compliance with regulatory standards in research settings, while pharmacists are healthcare providers responsible for dispensing medications and advising patients. Both roles require specialized knowledge but serve different functions within the healthcare and research industries.

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Glp jobs near you
Infographic showing various Glp job openings in the United States as of September 2026, with employment types broken down into 73% Full Time, 9% Part Time, and 18% Contract. Highlights an 82% In-person, 9% Hybrid, and 9% Remote job distribution, with an average salary of $47,622 per year, or $22.9 per hour.

Director of Quality Assurance, GLP QAU

Solana Beach, CA

RPM ReSearch
Recruiting and Staffing Services • 11 - 50 employees
Learn more about RPM ReSearchexternal

Full-time

Re-posted 6 days ago

Key responsibilities

  • Establish and lead the Quality Assurance Unit (QAU) to oversee nonclinical in vivo research and surgical studies.

  • Develop and implement SOPs, policies, and procedures to ensure GLP compliance and regulatory adherence across the facility.

  • Provide regulatory and quality oversight of in vivo preclinical studies, ensuring compliance with GLP regulations and animal welfare standards.

Job description

Director, GLP Quality Assurance & Compliance


Building a Culture of Quality & Compliance in a Leading In Vivo Research Facility


Company Overview


We are a pioneering research organization dedicated to translational medicine, bridging the gap between research and real-world applications to improve human health. As we expand our in vivo research capabilities, including a variety of preclinical studies, we are seeking an experienced Director, GLP Quality Assurance & Compliance to establish and lead a Quality Assurance Unit (QAU). This role will be critical in ensuring full Good Laboratory Practice (GLP) compliance and fostering a culture of quality across all research operations.


Position Overview


The Director, GLP Quality Assurance & Compliance will design, implement, and oversee a Quality Assurance Unit (QAU) that ensures research integrity and compliance with GLP regulations, FDA, USDA, AALAC and 21CFR Part 11 standards. The organiztion will start out on a paper based system and eventually move to a system like Pristima or Provantis. This role will be starting out from a fresh, bare facility and brought up to full compliance.  Reporting to the Test Faciliyt Manager, this leader will develop policies, oversee audits, and guide the organization through regulatory inspections. Additionally, they will play a key role in supporting in vivo research protocols and procedures procedures, ensuring that all processes align with in vivo and in vitro GLP studies and animal welfare regulations.


Key Responsibilities


1. Establishing & Leading the Quality Assurance Unit (QAU)

  • Develop and implement the Quality Assurance Unit (QAU) to provide independent oversight of nonclinical in vivo research and surgical studies.
  • Establish robust SOPs, policies, and procedures to align the entire facility with GLP principles and regulatory best practices of an in vivo and in vitro preclinical testing facility.
  • Design a structured audit program, including facility inspections, process reviews, data integrity assessments, and study audits to drive continuous improvement.
  • Ensure that all study documentation, electronic records, and data management systems adhere to 21CFR Part 11 and GLP-compliant guidelines.
  • Develop mechanisms for root cause analysis and Corrective and Preventative Actions (CAPAs) to address compliance gaps.


2. Quality Oversight of In Vivo and In Vitro Research Operations

  • Provide regulatory and quality oversight of in vivo preclinical studies, ensuring adherence to GLP regulations and animal welfare standards (USDA, OLAW, AALAC, IACUC).
  • Implement QA/QC processes for research and surgical procedures, ensuring proper sterility controls, aseptic technique documentation, and procedural compliance.
  • Work with veterinary and scientific staff to enhance procedural accuracy, maintain study integrity, and prevent deviations from protocols.
  • Ensure all study personnel, veterinary teams, and surgical staff are trained on GLP principles, and ethical research conduct.
  • Oversee the implementation of a data integrity program for preclinical research, including audit trails, validation procedures, and security measures for electronic records.


3. Regulatory Compliance & Risk Management

  • Serve as the primary regulatory liaison for FDA, USDA, and external auditors, ensuring the facility is always inspection-ready.
  • Maintain full separation and independence from study personnel, ensuring unbiased quality assurance and compliance verification.
  • Identify and mitigate compliance risks, reporting critical quality issues to senior leadership and advising on remediation strategies.


4. Team Leadership, Training & Continuous Improvement

  • Recruit, train, and develop a high-performing QAU team, including QA auditors and compliance specialists to support facility-wide GLP adherence.
  • Implement internal training programs to foster a culture of quality awareness, ensuring all personnel understand GLP expectations and regulatory requirements.
  • Collaborate with IT and software development teams to implement electronic systems that support GLP compliance and data security.
  • Design and implement a paper based system to serve as the backbone for a future electronic system. 
  • Monitor emerging regulatory trends and continuously refine QA/QC programs to maintain best-in-class compliance practices.


Qualifications


Education & Experience

  • Bachelor’s degree in a scientific discipline (Biology, Pharmacology, Chemistry, Veterinary Sciences, etc.); advanced degree (DVM, PhD, MD) preferred.
  • 8+ years of GLP-regulated experience in a preclinical research, contract research organization (CRO), or biopharmaceutical setting.
  • 4+ years in GLP quality assurance, with a demonstrated ability to build and lead a QAU.
  • 2+ years of managerial or supervisory experience in quality assurance, regulatory affairs, or compliance oversight.


Technical & Leadership Competencies

  • Expertise in GLP compliance with a strong understanding of 21CFR Part 11, electronic records/data integrity, and regulatory expectations.
  • Experience developing and implementing quality programs as well as daily execution for in vivo preclinical research, surgical procedures, and regulatory compliance.
  • Strong analytical and problem-solving skills to assess complex compliance issues and recommend effective solutions.
  • Exceptional communication, leadership, and cross-functional collaboration skills.
  • Ability to thrive in a fast-paced, evolving research environment, balancing compliance demands with operational efficiency.


What We Offer

  • A pivotal role in shaping GLP compliance and preclinical research quality at a cutting-edge research facility.
  • Competitive compensation and benefits package.
  • Professional development and training opportunities to enhance expertise in regulatory compliance and quality systems.
  • A collaborative, innovative work environment dedicated to scientific excellence and ethical research.


Join Us!


If you are an experienced GLP Quality Leader with a passion for building world-class quality programs and ensuring compliance in in vivo research non-clinical studies, we invite you to apply. Help us advance preclinical science while upholding the highest standards of quality, integrity, and regulatory excellence.